Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17265513 | 0.925 | 0.160 | 20 | 41203988 | missense variant | T/C | snv | 0.14 | 0.14 | 6 | |
rs11603334 | 1.000 | 0.080 | 11 | 72721940 | 5 prime UTR variant | G/A | snv | 0.12 | 5 | ||
rs11605924 | 1.000 | 0.080 | 11 | 45851540 | intron variant | A/C | snv | 0.39 | 5 | ||
rs17168486 | 1.000 | 0.080 | 7 | 14858657 | intron variant | C/T | snv | 0.18 | 5 | ||
rs2851682 | 11 | 61848540 | intron variant | A/G | snv | 9.9E-02 | 5 | ||||
rs11672660 | 19 | 45676926 | intron variant | C/T | snv | 0.18 | 0.17 | 5 | |||
rs7651090 | 0.925 | 0.080 | 3 | 185795604 | intron variant | A/G | snv | 0.39 | 5 | ||
rs11558471 | 1.000 | 0.080 | 8 | 117173494 | 3 prime UTR variant | A/G | snv | 0.25 | 5 | ||
rs7944584 | 1.000 | 0.080 | 11 | 47314769 | intron variant | A/T | snv | 0.19 | 5 | ||
rs11920090 | 1.000 | 0.040 | 3 | 170999732 | intron variant | T/A | snv | 0.20 | 5 | ||
rs3802177 | 1.000 | 0.080 | 8 | 117172786 | 3 prime UTR variant | G/A | snv | 0.24 | 5 | ||
rs10885122 | 1.000 | 0.080 | 10 | 111282335 | intergenic variant | T/G | snv | 0.71 | 4 | ||
rs11257655 | 1.000 | 0.080 | 10 | 12265895 | TF binding site variant | C/T | snv | 0.23 | 4 | ||
rs13023194 | 0.925 | 0.120 | 2 | 27744393 | intergenic variant | G/A;C | snv | 4 | |||
rs1483121 | 1.000 | 0.080 | 11 | 48311808 | downstream gene variant | G/A | snv | 9.7E-02 | 4 | ||
rs2191349 | 1.000 | 0.080 | 7 | 15024684 | intergenic variant | G/T | snv | 0.54 | 4 | ||
rs4502156 | 1.000 | 0.080 | 15 | 62090956 | intergenic variant | T/C | snv | 0.55 | 4 | ||
rs853789 | 2 | 168944978 | intron variant | A/G;T | snv | 0.75 | 4 | ||||
rs2877716 | 3 | 123375604 | intron variant | T/C | snv | 0.76 | 4 | ||||
rs1552224 | 1.000 | 0.080 | 11 | 72722053 | 5 prime UTR variant | A/C | snv | 0.12 | 4 | ||
rs6975024 | 7 | 44192287 | intron variant | T/C | snv | 0.14 | 4 | ||||
rs780110 | 0.925 | 0.120 | 2 | 27462521 | intron variant | G/A | snv | 0.56 | 4 | ||
rs4665965 | 0.925 | 0.120 | 2 | 27313513 | intron variant | T/A;C | snv | 4 | |||
rs2305929 | 1.000 | 0.040 | 2 | 27891044 | intron variant | A/G | snv | 0.14 | 4 | ||
rs17762454 | 0.925 | 0.120 | 6 | 7212967 | non coding transcript exon variant | C/T | snv | 0.25 | 4 |